Abstract
(1) Objective: To review the criteria proposed by Cerero-Lapiedra et al. and to retrospectively identify the under-diagnosed disease in patients diagnosed with proliferative verrucous leukoplakia. (2) Materials and methods: In this study, we included patients who were diagnosed with leukoplakia (histological label consistent with the clinical diagnosis, n = 95), and cases with a final diagnosis within the spectrum of proliferative verrucous leukoplakia (n = 110) as defined by Batsakis et al. We applied the criteria proposed by Cerero-Lepiedra et al. to screen for the possible cases of proliferative verrucous leukoplakia. (3) Results: Although many of our patients satisfied specific isolated criteria, only 11 cases satisfied specific combinations of the guidelines to satisfy a diagnosis of proliferative verrucous leukoplakia. However, due to the lack of follow-up data, the disease is not confirmed in these 11 cases. (4) Conclusion: A limited number of cases of proliferative verrucous leukoplakia were diagnosed using the criteria given by Cerero-Lapiedra et al. The true natural history of the disease could not be studied due to the lack of follow-up data. (5) Clinical relevance: Proliferative verrucous leukoplakia presenting as hyperkeratosis or mild epithelial dysplasia are often not followed up, and they subsequently transform into carcinoma. Thus, clinicians must be vigilant whenever they encounter leukoplakia, especially with multifocal presentations. In such cases, the follow-up data are the key to understanding the true nature of the disease entity.
Highlights
Proliferative verrucous leukoplakia (PVL), a unique form of leukoplakia, was first reported by Hansen et al [1] in a long-term study of 30 patients
We aim to identify the possible under- or over-diagnosed PVL cases retrospectively
PVL progresses from an isolated leukoplakia to become multi-focal confluent or isolated exophytic/verrucous lesions
Summary
Proliferative verrucous leukoplakia (PVL), a unique form of leukoplakia, was first reported by Hansen et al [1] in a long-term study of 30 patients. PVL clinically commences as an isolated homogenous leukoplakia lesion, microscopically manifesting as simple hyperkeratosis without dysplasia. The lesions spread to affect other locations. These lesions tend to recur and become exophytic with or without an erythematous component. Depending upon the severity of the lesion under microscope, PVL is histopathologically graded from 0 to 10. The histopathological spectrum ranges as simple hyperkeratosis, varying grades of epithelial dysplasia, verrucous hyperplasia (VH), verrucous carcinoma (VC), papillary squamous cell carcinoma (PSCC), and oral squamous cell carcinoma (OSCC)
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